P11T (p.Pro11Thr) variant of NPM1 (Nucleophosmin)
P11T (p.Pro11Thr) in NPM1 (Nucleophosmin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.37 / 1. The record also includes population frequency data, published literature, and structural context.
P11T (p.Pro11Thr) variant details
- p.Pro11Thr
- gnomAD 5-171387979-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.365
- REVEL 0.18
- CADD 22.80
- PolyPhen-2 0.42
- SIFT 0.09
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available